Version: 8.0.0Date: Tue Jan 28 2025
Allele/Variant
rs763885620
- Species
- Homo sapiens
- Symbol
- rs763885620
- Category
- Variant
- Variant type
- SNP
- Overlaps
- UBE2M
- Location
- 19:58557107
- Nucleotide Change
- G>T
- Most Severe Consequence
- See all consequences
- missense variant
- HGVS.g name
- NC_000019.10:g.58557107G>T
- HGVS.c name
- ENSEMBL:ENST00000253023.8:c.160C>A
- ENSEMBL:ENST00000593801.1:n.43C>A
- HGVS.p name
- ENSP00000253023:p.Pro54Thr
- NP_003960:p.Pro54Thr
- Synonyms
- Not Available
- Notes
- Not Available
- Cross references
- Not Available
- References
- Not Available
- Genome location
- Chr19:58555712...58558954 (3.24 kb)
- Assembly version
- Not Available
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